Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic epidemiology of Creutzfeldt-Jakob disease in Europe.

Revue neurologique - 1 Jul 2001

Abstract excerpt

The prion protein gene was studied in patients with definite or probable Creutzfeldt-Jakob disease (CJD) registered by national CJD units of 6 European countries. The role of genetic factors in CJD was also investigated by comparing the frequencies of a family history of dementia and Parkinson's disease in CJD cases and matched controls. Codon 129 genotype was examined in 337 CJD cases of whom 73.2 p. 100 were...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Codon
Share to Creutzfeldt-Jakob Syndrome
Share to Dementia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Europe

Share to Genetic Carrier Screening

Share to Incidence

Share to Parkinson Disease

Share to Prions

Source

Identifiers

PMID: 11458182

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic epidemiology of Creutzfeldt-Jakob disease in Europe.PMID 11458182Read ↗

Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies.Semantic proximity Read ↗

Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob Disease phenotype.Semantic proximity Read ↗

PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.Semantic proximity Read ↗

Genetic Creutzfeldt-Jakob disease.Semantic proximity Read ↗

Prion disease genetics.Semantic proximity Read ↗

Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.Semantic proximity Read ↗

A French cluster of Creutzfeldt-Jakob disease: a molecular analysis.Semantic proximity Read ↗

Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease.Semantic proximity Read ↗

Creutzfeldt-Jakob disease in Hungary.Semantic proximity Read ↗

Genetic risk factors associated with Creutzfeld-Jakob disease in Slovenians and a rapid typing for PRNP codon 129 single nucleotide polymorphism.Semantic proximity Read ↗

Genetic studies in human prion diseases.Semantic proximity Read ↗

Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillance.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.